SG187883A1 - Pest control agent - Google Patents
Pest control agent Download PDFInfo
- Publication number
- SG187883A1 SG187883A1 SG2013011887A SG2013011887A SG187883A1 SG 187883 A1 SG187883 A1 SG 187883A1 SG 2013011887 A SG2013011887 A SG 2013011887A SG 2013011887 A SG2013011887 A SG 2013011887A SG 187883 A1 SG187883 A1 SG 187883A1
- Authority
- SG
- Singapore
- Prior art keywords
- group
- substituted
- halogen atom
- formula
- compound
- Prior art date
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- 241000607479 Yersinia pestis Species 0.000 title claims abstract description 181
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 96
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 68
- 150000001412 amines Chemical class 0.000 claims abstract description 35
- 230000000694 effects Effects 0.000 claims abstract description 31
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 20
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 10
- 150000001875 compounds Chemical class 0.000 claims description 335
- -1 or a Ci Chemical group 0.000 claims description 265
- 125000005843 halogen group Chemical group 0.000 claims description 224
- 125000000217 alkyl group Chemical group 0.000 claims description 173
- 238000000034 method Methods 0.000 claims description 85
- 229910052736 halogen Inorganic materials 0.000 claims description 47
- 150000002367 halogens Chemical class 0.000 claims description 45
- 150000003839 salts Chemical class 0.000 claims description 36
- 125000003545 alkoxy group Chemical group 0.000 claims description 34
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 34
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 30
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 30
- 239000007787 solid Substances 0.000 claims description 28
- 239000002689 soil Substances 0.000 claims description 22
- 125000001424 substituent group Chemical group 0.000 claims description 21
- 241000238876 Acari Species 0.000 claims description 20
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 19
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 18
- 241001465754 Metazoa Species 0.000 claims description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 16
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 16
- 229910052757 nitrogen Inorganic materials 0.000 claims description 15
- 239000000575 pesticide Substances 0.000 claims description 15
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 14
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 14
- 241000002163 Mesapamea fractilinea Species 0.000 claims description 13
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 13
- 230000003071 parasitic effect Effects 0.000 claims description 13
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- 241000282465 Canis Species 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- NWOFWGTYDVCXRD-UHFFFAOYSA-N n-[1-[(6-chloropyridin-3-yl)methyl]pyridin-2-ylidene]-2,2,3,3,3-pentafluoropropanamide Chemical compound FC(F)(F)C(F)(F)C(=O)N=C1C=CC=CN1CC1=CC=C(Cl)N=C1 NWOFWGTYDVCXRD-UHFFFAOYSA-N 0.000 claims description 10
- 125000004450 alkenylene group Chemical group 0.000 claims description 8
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 8
- 125000004419 alkynylene group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 8
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 7
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 7
- 241000258242 Siphonaptera Species 0.000 claims description 6
- 125000004414 alkyl thio group Chemical group 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 6
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- 235000015097 nutrients Nutrition 0.000 claims description 6
- 125000006584 (C3-C10) heterocycloalkyl group Chemical group 0.000 claims description 5
- 125000005330 8 membered heterocyclic group Chemical group 0.000 claims description 5
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- DHQKLWKZSFCKTA-UHFFFAOYSA-N n-[1-[(6-chloropyridin-3-yl)methyl]pyridin-2-ylidene]-2,2,2-trifluoroacetamide Chemical compound FC(F)(F)C(=O)N=C1C=CC=CN1CC1=CC=C(Cl)N=C1 DHQKLWKZSFCKTA-UHFFFAOYSA-N 0.000 claims description 5
- 125000004076 pyridyl group Chemical group 0.000 claims description 5
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 5
- 239000001963 growth medium Substances 0.000 claims description 4
- ABFADXMVCUMADD-UHFFFAOYSA-N 2,2,2-trifluoro-n-[1-[(6-fluoropyridin-3-yl)methyl]pyridin-2-ylidene]acetamide Chemical compound C1=NC(F)=CC=C1CN1C(=NC(=O)C(F)(F)F)C=CC=C1 ABFADXMVCUMADD-UHFFFAOYSA-N 0.000 claims description 3
- 230000001939 inductive effect Effects 0.000 claims description 2
- 239000000126 substance Substances 0.000 abstract description 62
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- 239000002585 base Substances 0.000 description 62
- 239000000243 solution Substances 0.000 description 62
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- 230000015572 biosynthetic process Effects 0.000 description 58
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- 239000011541 reaction mixture Substances 0.000 description 45
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 44
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 44
- 238000009472 formulation Methods 0.000 description 44
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 43
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 39
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- 238000005160 1H NMR spectroscopy Methods 0.000 description 33
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- 229910000027 potassium carbonate Inorganic materials 0.000 description 32
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Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
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| JP2010194584 | 2010-08-31 | ||
| PCT/JP2011/069352 WO2012029672A1 (fr) | 2010-08-31 | 2011-08-26 | Agent de lutte contre des organismes nuisibles |
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| SG187883A1 true SG187883A1 (en) | 2013-03-28 |
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| SG2013011887A SG187883A1 (en) | 2010-08-31 | 2011-08-26 | Pest control agent |
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| WO (1) | WO2012029672A1 (fr) |
| ZA (1) | ZA201301156B (fr) |
Families Citing this family (343)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2984930T3 (pl) * | 2010-08-31 | 2019-03-29 | Meiji Seika Pharma Co., Ltd. | Środek do zwalczania szkodników |
| EP3318554B1 (fr) | 2011-08-26 | 2021-11-03 | Meiji Seika Pharma Co., Ltd. | Procédé de fabrication d'un agent de contrôle de nuisibles |
| CN112244015B (zh) * | 2012-02-29 | 2022-05-17 | 株式会社Mmag | 包括新型亚氨基吡啶衍生物的有害物防治组合物 |
| CN104220424A (zh) * | 2012-02-29 | 2014-12-17 | 明治制果药业株式会社 | 具有2-亚氨基的含氮杂环衍生物以及包含它的害虫防治剂 |
| WO2013144088A1 (fr) | 2012-03-29 | 2013-10-03 | Basf Se | Composés hétéro-bicycliques n-substitués et dérivés pour la lutte contre animaux nuisibles |
| WO2013144223A1 (fr) | 2012-03-30 | 2013-10-03 | Basf Se | Composés de pyrimidinylidène n-substitués et dérivés destinés à lutter contre les animaux nuisibles |
| ES2626360T3 (es) | 2012-03-30 | 2017-07-24 | Basf Se | Compuestos de piridinilideno tiocarbonilo N-sustituidos y su uso para combatir plagas de animales |
| CN104487439B (zh) | 2012-05-24 | 2017-06-09 | 巴斯夫欧洲公司 | N‑硫代邻氨基苯甲酰胺化合物及其作为杀害虫剂的用途 |
| MX2014015265A (es) | 2012-06-14 | 2015-08-12 | Basf Se | Metodos plaguicidas que utilizan compuestos de 3-piridiltiazol sustituido y derivados para combatir plagas de animales. |
| WO2014005982A1 (fr) | 2012-07-05 | 2014-01-09 | Bayer Cropscience Ag | Associations de principes actifs insecticides et fongicides |
| AR093771A1 (es) | 2012-10-01 | 2015-06-24 | Basf Se | Metodo para controlar insectos resistentes a insecticidas |
| KR20150067270A (ko) | 2012-10-01 | 2015-06-17 | 바스프 에스이 | 안트라닐아미드 화합물을 포함하는 살충적으로 활성인 혼합물 |
| AR093772A1 (es) | 2012-10-01 | 2015-06-24 | Basf Se | Metodo para controlar insectos resistentes a insecticidas moduladores de rianodina |
| WO2014053401A2 (fr) | 2012-10-01 | 2014-04-10 | Basf Se | Procédé d'amélioration de la santé des plantes |
| WO2014053407A1 (fr) | 2012-10-01 | 2014-04-10 | Basf Se | Composés n-thio-anthranilamides et leur utilisation en tant que pesticides |
| AR093828A1 (es) | 2012-10-01 | 2015-06-24 | Basf Se | Mezclas activas como plaguicidas, que comprenden compuestos de antranilamida |
| EP2903437A1 (fr) | 2012-10-01 | 2015-08-12 | Basf Se | Utilisation de composés de n-thio-anthranilamide sur des plantes cultivées |
| WO2014079772A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
| WO2014079773A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
| CN104902756B (zh) | 2012-11-22 | 2018-11-27 | 巴斯夫公司 | 农药混合物 |
| WO2014079804A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
| WO2014079774A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
| WO2014079770A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
| WO2014079820A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Utilisation de composés d'anthranilamides pour réduire les infections virales véhiculées par les insectes |
| WO2014079841A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
| WO2014079766A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
| CA2889775A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Corporation | Melanges pesticides |
| WO2014079813A1 (fr) | 2012-11-23 | 2014-05-30 | Basf Se | Mélanges pesticides |
| WO2014079752A1 (fr) | 2012-11-23 | 2014-05-30 | Basf Se | Mélanges pesticides |
| EP2984074A1 (fr) | 2012-12-14 | 2016-02-17 | Basf Se | Composés de malononitrile pour lutter contre les nuisibles d'origine animale |
| CN105189489A (zh) | 2012-12-27 | 2015-12-23 | 巴斯夫欧洲公司 | 用于防除无脊椎动物害虫的带有亚胺或亚胺衍生取代基的2-(吡啶-3-基)-5-杂芳基噻唑化合物 |
| WO2014128136A1 (fr) | 2013-02-20 | 2014-08-28 | Basf Se | Composés d'anthranilamide et leur utilisation comme pesticides |
| WO2014170300A1 (fr) | 2013-04-19 | 2014-10-23 | Basf Se | Composés et dérivés d'acyliminopyridine n-substitués pour lutter contre des animaux nuisibles |
| WO2014192717A1 (fr) * | 2013-05-27 | 2014-12-04 | Meiji Seikaファルマ株式会社 | Agents de lutte contre les parasites des abeille mellifères et méthode de lutte contre les parasites des abeilles mellifères dans lesquelles ces derniers sont utilisés |
| US20160145222A1 (en) | 2013-06-21 | 2016-05-26 | Basf Se | Methods for Controlling Pests in Soybean |
| AU2014292164C1 (en) | 2013-07-15 | 2018-09-27 | Basf Se | Pesticide compounds |
| WO2015028630A1 (fr) * | 2013-08-30 | 2015-03-05 | Basf Se | Composés de pyridylidène n-substitués et leurs dérivés utilisables pour lutter contre les animaux nuisibles |
| CN105593223A (zh) * | 2013-09-19 | 2016-05-18 | 巴斯夫欧洲公司 | N-丙烯酰亚氨基杂环化合物 |
| US10206397B2 (en) | 2013-09-19 | 2019-02-19 | Basf Se | N-acylimino heterocyclic compounds |
| WO2015055554A1 (fr) | 2013-10-14 | 2015-04-23 | Bayer Cropscience Ag | Principe actif pour le traitement des semences et du sol |
| UY35772A (es) | 2013-10-14 | 2015-05-29 | Bayer Cropscience Ag | Nuevos compuestos plaguicidas |
| WO2015055505A1 (fr) * | 2013-10-14 | 2015-04-23 | Bayer Cropscience Ag | Principe actif pour la lutte contre les punaises |
| WO2015055497A1 (fr) | 2013-10-16 | 2015-04-23 | Basf Se | Composés pesticides de pyrazole substitué |
| MX386864B (es) | 2013-10-18 | 2025-03-19 | Basf Agrochemical Products Bv | Uso de derivado de carboxamida activo como plaguicida en métodos de aplicación y tratamiento de suelo y semillas. |
| WO2015059088A1 (fr) | 2013-10-23 | 2015-04-30 | Bayer Cropscience Ag | Dérivés de chinoxaline substitués servant d'agent de lutte antiparasitaire |
| EP3071560B1 (fr) * | 2013-11-22 | 2018-01-10 | Basf Se | Composés hétérocycliques n-acylimino |
| CN105829296A (zh) | 2013-12-18 | 2016-08-03 | 巴斯夫欧洲公司 | 带有亚胺衍生的取代基的唑类化合物 |
| WO2015091649A1 (fr) | 2013-12-18 | 2015-06-25 | Basf Se | Composés hétérocycliques de type imino n-substitués |
| KR20160104065A (ko) | 2014-01-03 | 2016-09-02 | 바이엘 애니멀 헬스 게엠베하 | 농약으로서의 신규 피라졸릴헤테로아릴아미드 |
| WO2015104422A1 (fr) | 2014-01-13 | 2015-07-16 | Basf Se | Composés dihydrothiophène dans la lutte contre des nuisibles invertébrés |
| TW201612161A (en) | 2014-01-20 | 2016-04-01 | Bayer Cropscience Ag | Quinoline derivatives as insecticides and acaricides |
| WO2015137216A1 (fr) * | 2014-03-10 | 2015-09-17 | Meiji Seikaファルマ株式会社 | Procede de production de derive de 2-acyliminopyridine |
| JP2017510588A (ja) * | 2014-03-27 | 2017-04-13 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 無脊椎有害生物を防除するためのn−アシルイミノ複素環式化合物 |
| JP6434048B2 (ja) | 2014-04-02 | 2018-12-05 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 農薬としてのヘテロ環式化合物 |
| CN106661022B (zh) | 2014-05-08 | 2018-05-04 | 拜耳作物科学股份公司 | 作为杀线虫剂的吡唑并吡啶磺酰胺 |
| BR112016028404A2 (pt) | 2014-06-05 | 2018-07-03 | Bayer Cropscience Aktiengesellschaft | compostos bicíclicos como pesticidas |
| WO2016001119A1 (fr) | 2014-07-01 | 2016-01-07 | Bayer Cropscience Aktiengesellschaft | Associations de principes actifs insecticides et fongicides |
| WO2016001122A1 (fr) * | 2014-07-01 | 2016-01-07 | Bayer Cropscience Aktiengesellschaft | Procédés pour améliorer la croissance de végétaux |
| WO2016001125A1 (fr) * | 2014-07-01 | 2016-01-07 | Bayer Cropscience Aktiengesellschaft | Combinaisons de composés actifs et procédés pour protéger le matériau de propagation des plantes |
| WO2016001121A1 (fr) * | 2014-07-01 | 2016-01-07 | Bayer Cropscience Aktiengesellschaft | Procédé pour une utilisation améliorée du potentiel de production de plantes transgéniques |
| WO2016001129A1 (fr) | 2014-07-01 | 2016-01-07 | Bayer Cropscience Aktiengesellschaft | Compositions insecticides améliorées |
| WO2016001120A1 (fr) * | 2014-07-01 | 2016-01-07 | Bayer Cropscience Aktiengesellschaft | Association de principes actifs insecticides |
| WO2016005276A1 (fr) * | 2014-07-07 | 2016-01-14 | Bayer Cropscience Aktiengesellschaft | Procédé de préparation de composés fluorés d'iminopyridine |
| JP2017521441A (ja) | 2014-07-15 | 2017-08-03 | バイエル・アニマル・ヘルス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Animal Health Gmbh | 有害生物防除剤としてのアリール−トリアゾリルピリジン類 |
| BR112017005140A2 (pt) | 2014-10-06 | 2018-01-23 | Basf Se | compostos, mistura, composição, métodos para a proteção de culturas e para o combate ou controle de praga de invertebrados, método não terapêutico para o tratamento de animais infestados ou infectados por parasitas e semente |
| WO2016055096A1 (fr) | 2014-10-07 | 2016-04-14 | Bayer Cropscience Ag | Procédé de traitement de semence de riz |
| BR112017009513A2 (pt) | 2014-11-06 | 2018-02-06 | Basf Se | utilização de um composto heterobicíclico, utilização dos compostos i, compostos, composição agrícola ou veterinária, método para o combate ou controle de pragas, método para a proteção de culturas e sementes |
| AR102942A1 (es) | 2014-12-11 | 2017-04-05 | Bayer Cropscience Ag | Derivados de arilsulfuro y arilsulfóxido de cinco miembros c-n-conectados, como plaguicidas |
| EP3081085A1 (fr) | 2015-04-14 | 2016-10-19 | Bayer CropScience AG | Procédé d'amélioration de précocité dans le coton |
| UY36548A (es) | 2015-02-05 | 2016-06-01 | Bayer Cropscience Ag | Derivados heterocíclicos condensados bicíclicos sustituidos por 2-(het)arilo como pesticidas |
| UY36547A (es) | 2015-02-05 | 2016-06-01 | Bayer Cropscience Ag | Derivados heterocíclicos condensados bicíclicos sustituidos por 2-(het)arilo como pesticidas |
| EP3253209A1 (fr) | 2015-02-06 | 2017-12-13 | Basf Se | Composés de pyrazole utilisés en tant qu'inhibiteurs de nitrification |
| TWI702212B (zh) | 2015-02-09 | 2020-08-21 | 德商拜耳作物科學股份有限公司 | 作為除害劑之經取代的2-硫基咪唑基羧醯胺類 |
| WO2016128261A2 (fr) | 2015-02-11 | 2016-08-18 | Basf Se | Mélange pesticide comprenant un composé pyrazole, un insecticide et un fongicide |
| AU2016231174B2 (en) | 2015-03-10 | 2020-09-10 | Bayer Animal Health Gmbh | Pyrazolyl-derivatives as pest control agents |
| BR112017021450B1 (pt) | 2015-04-07 | 2021-12-28 | Basf Agrochemical Products B.V. | Métodos de controle de pragas, método de melhoria da saúde vegetal e semente revestida |
| BR112017021408B1 (pt) | 2015-04-08 | 2022-05-17 | Bayer Cropscience Aktiengesellschaft | Derivados de heterociclo bicíclico condensado, método para controlar pragas animais, e formulação agroquímica |
| WO2016174049A1 (fr) | 2015-04-30 | 2016-11-03 | Bayer Animal Health Gmbh | Combinaisons anti-parasitaires comprenant des composés à substitution halogène |
| MX2017014459A (es) | 2015-05-12 | 2018-03-16 | Basf Se | Compuestos de tioeter como inhibidores de la nitrificacion. |
| CN107835803A (zh) | 2015-05-13 | 2018-03-23 | 拜耳作物科学股份公司 | 杀昆虫的芳基吡咯烷、其制备方法及其作为试剂用于防治动物害虫的用途 |
| WO2016198613A1 (fr) | 2015-06-11 | 2016-12-15 | Basf Se | Composés n-(thio)acylimino |
| WO2016198611A1 (fr) | 2015-06-11 | 2016-12-15 | Basf Se | Composés hétérocycliques n-(thio)acylimino |
| JP6732877B2 (ja) | 2015-07-06 | 2020-07-29 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 殺虫剤としての複素環式化合物 |
| WO2017016883A1 (fr) | 2015-07-24 | 2017-02-02 | Basf Se | Procédé de préparation de composés cyclopentène |
| CN108137548A (zh) | 2015-08-07 | 2018-06-08 | 拜耳作物科学股份公司 | 作为农药的2-(杂)芳基取代的稠合杂环衍生物 |
| WO2017055386A1 (fr) | 2015-10-02 | 2017-04-06 | Basf Se | Utilisation de composés imino comportant un substituant 2-chloropyrimidine-5-yle comme agents de lutte contre les ravageurs |
| US10550116B2 (en) | 2015-10-26 | 2020-02-04 | Bayer Cropscience Aktiengesellschaft | Fused bicyclic heterocycle derivatives as pesticides |
| PL3383183T3 (pl) | 2015-11-30 | 2020-11-16 | Basf Se | Kompozycje zawierające cis-jasmon i bacillus amyloliquefaciens |
| WO2017093180A1 (fr) | 2015-12-01 | 2017-06-08 | Bayer Cropscience Aktiengesellschaft | Dérivés hétérocycles bicycliques condensés utilisés en tant que produits de lutte antiparasitaire |
| AU2016363632A1 (en) | 2015-12-03 | 2018-06-07 | Bayer Cropscience Aktiengesellschaft | Mesoionic halogenated 3-(acetyl)-1-((1,3-thiazol-5-yl)methyl)-1h-imidazo(1,2-a)pyridin-4-ium-2-olate derivatives and related compounds as insecticides |
| JPWO2017104692A1 (ja) * | 2015-12-15 | 2018-09-27 | Meiji Seikaファルマ株式会社 | シロアリ防除剤 |
| PH12018501138B1 (en) | 2015-12-29 | 2023-09-27 | Mmag Co Ltd | Pest control composition including iminopyridine derivative |
| CA3013963A1 (fr) | 2016-02-11 | 2017-08-17 | Bayer Cropscience Aktiengesellschaft | 2-oxyimidazolyl-carboxamides substitues utilises comme pesticides |
| BR112018016360A2 (pt) | 2016-02-11 | 2018-12-18 | Bayer Cropscience Aktiengesellschaft | 2-(het)arilimidazolilcarboxiamidas substituídas como pesticidas |
| WO2017144341A1 (fr) | 2016-02-23 | 2017-08-31 | Bayer Cropscience Aktiengesellschaft | Dérivés hétérocycliques bicycliques condensés utilisés en tant que produits de lutte antiparasitaire |
| EP3210468A1 (fr) | 2016-02-26 | 2017-08-30 | Bayer CropScience Aktiengesellschaft | Compositions sans solvant pour agents actifs a bas point de fusion |
| WO2017153217A1 (fr) | 2016-03-09 | 2017-09-14 | Basf Se | Dérivés spirocycliques |
| BR112018068042A2 (pt) | 2016-03-11 | 2019-01-08 | Basf Se | métodos para controlar pragas de plantas, material de propagação de planta e uso de um ou mais compostos de fórmula i |
| EP3429355B1 (fr) | 2016-03-15 | 2020-02-05 | Bayer CropScience AG | Sulfonylamides substitues pour la lutte contre les ravageurs |
| JP2019513700A (ja) | 2016-03-16 | 2019-05-30 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 殺有害生物剤及び植物保護剤としてのn−(シアノベンジル)−6−(シクロプロピル−カルボニルアミノ)−4−(フェニル)−ピリジン−2−カルボキサミド誘導体及び関連する化合物 |
| CA3015934A1 (fr) | 2016-04-01 | 2017-10-05 | Basf Se | Composes bicycliques |
| WO2017174414A1 (fr) | 2016-04-05 | 2017-10-12 | Bayer Cropscience Aktiengesellschaft | Dérivés de naphtaline utilisés comme agents de lutte contre les nuisibles |
| KR102467347B1 (ko) | 2016-04-15 | 2022-11-14 | 바이엘 애니멀 헬스 게엠베하 | 피라졸로피리미딘 유도체 |
| PE20190215A1 (es) | 2016-04-25 | 2019-02-07 | Bayer Cropscience Ag | 2-alquilimidazolilcarboxamidas sustituidas como plaguicidas |
| EP3241830A1 (fr) | 2016-05-04 | 2017-11-08 | Bayer CropScience Aktiengesellschaft | Derivés de bicycles condensés hétérocycliques utilisés comme pesticides |
| WO2017198450A1 (fr) | 2016-05-15 | 2017-11-23 | Bayer Cropscience Nv | Procédé pour accroître le rendement du maïs |
| WO2017198449A1 (fr) | 2016-05-15 | 2017-11-23 | Bayer Cropscience Nv | Procédé pour accroître le rendement chez les brassicaceae |
| EP3245865A1 (fr) | 2016-05-17 | 2017-11-22 | Bayer CropScience Aktiengesellschaft | Procédé pour augmenter le rendement dans des brassicacées |
| WO2017198452A1 (fr) | 2016-05-16 | 2017-11-23 | Bayer Cropscience Nv | Procédé pour accroître le rendement du soja |
| WO2017198453A1 (fr) | 2016-05-16 | 2017-11-23 | Bayer Cropscience Nv | Procédé d'augmentation du rendement dans la pomme de terre, la tomate ou la luzerne |
| WO2017198451A1 (fr) | 2016-05-17 | 2017-11-23 | Bayer Cropscience Nv | Procédé pour augmenter le rendement dans des céréales à grains fins telles que le blé et le riz |
| WO2017198455A2 (fr) | 2016-05-17 | 2017-11-23 | Bayer Cropscience Nv | Procédé pour accroître le rendement de plantes bêta spp. |
| WO2017198454A1 (fr) | 2016-05-17 | 2017-11-23 | Bayer Cropscience Nv | Procédé pour accroître le rendement du coton |
| AU2017267129A1 (en) | 2016-05-18 | 2018-11-22 | Basf Se | Capsules comprising benzylpropargylethers for use as nitrification inhibitors |
| US10653136B2 (en) | 2016-07-11 | 2020-05-19 | Covestro Llc | Aqueous compositions for treating seeds, seeds treated therewith, and methods for treating seeds |
| US10750750B2 (en) | 2016-07-11 | 2020-08-25 | Covestro Llc | Aqueous compositions for treating seeds, seeds treated therewith, and methods for treating seeds |
| US10653135B2 (en) | 2016-07-11 | 2020-05-19 | Covestro Llc | Methods for treating seeds with an aqueous composition and seeds treated therewith |
| MX2019000512A (es) | 2016-07-12 | 2019-05-02 | Bayer Cropscience Ag | Compuestos biciclicos como plaguicidas. |
| MX2019000793A (es) | 2016-07-19 | 2019-06-20 | Bayer Cropscience Ag | Derivados de heterociclos biciclicos condensados como pesticidas. |
| UA127919C2 (uk) | 2016-07-29 | 2024-02-14 | Баєр Кропсаєнс Акціенгезельшафт | Препарат, який включає корисний штам p. bilaii та тальк, для застосування в обробці насіння |
| AR109107A1 (es) | 2016-07-29 | 2018-10-31 | Bayer Cropscience Ag | Compuestos halógeno(tio)acilo sustituidos |
| AU2017309725A1 (en) | 2016-08-10 | 2019-02-21 | Bayer Cropscience Aktiengesellschaft | Substituted 2-heterocyclyl imidazolyl-carboxamides as pest control agents |
| EP3497102B1 (fr) | 2016-08-15 | 2022-12-07 | Bayer CropScience Aktiengesellschaft | Dérivés d'hétérocyclène bicycliques condensés en tant que pesticides |
| EP4089075A1 (fr) | 2016-09-16 | 2022-11-16 | MMAG Co., Ltd. | Procédé de production optimisé pour un agent de lutte contre les nuisibles |
| EP3515921B1 (fr) | 2016-09-19 | 2021-10-27 | Bayer CropScience Aktiengesellschaft | Dérivés de pyrazolo[1,5-a]pyridine et leur utilisation en tant que pesticides |
| BR112019006985B1 (pt) | 2016-10-06 | 2023-02-07 | Bayer Cropscience Aktiengesellschaft | Derivados de heterocíclicos fundidos bicíclicos substituídos por 2- (het)arila, seu uso, formulação agroquímica, e método para controle de pragas animais |
| WO2018065288A1 (fr) | 2016-10-07 | 2018-04-12 | Bayer Cropscience Aktiengesellschaft | Dérivés de 2-[2-phényl-1-(sulfonylméthyl)vinyl]-imidazo[4,5-b]pyridine et composés apparentés utilisés comme pesticides en protection des plantes |
| EP3525588B1 (fr) | 2016-10-14 | 2024-04-24 | PI Industries Ltd | Phénylamidines 4-substituées et leur application pour la protection de plantes utiles par le combat de microorganismes indésirables |
| EP3525589B1 (fr) | 2016-10-14 | 2023-12-06 | PI Industries Ltd | Phénylamidines 4-arylamino substituées et leur application pour la protection de plantes utiles par le combat de microorganismes indésirables |
| TW201822637A (zh) | 2016-11-07 | 2018-07-01 | 德商拜耳廠股份有限公司 | 用於控制動物害蟲的經取代磺醯胺類 |
| CN109890793B (zh) | 2016-11-11 | 2022-11-18 | 拜耳动物保健有限责任公司 | 新的抗蠕虫药喹啉-3-甲酰胺衍生物 |
| KR20190084310A (ko) | 2016-11-23 | 2019-07-16 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 살충제로서의 2-[3-(알킬술포닐)-2H-인다졸-2-일]-3H-이미다조[4,5-b]피리딘 유도체 및 유사한 화합물 |
| EP3400801A1 (fr) | 2017-05-10 | 2018-11-14 | Bayer CropScience Aktiengesellschaft | Effet sur la santé de plantes de lilacinum purpureocillium |
| BR112019012262A2 (pt) | 2016-12-16 | 2019-12-03 | Bayer Ag | imidazopiridinas mesoiônicas para uso como inseticidas |
| CN110382493A (zh) | 2016-12-16 | 2019-10-25 | 拜耳农作物科学股份公司 | 作为农药的噻二唑衍生物 |
| US20200077658A1 (en) | 2016-12-16 | 2020-03-12 | Basf Se | Pesticidal Compounds |
| WO2018116072A1 (fr) | 2016-12-20 | 2018-06-28 | Pi Industries Ltd. | Composés hétérocycliques |
| WO2018116073A1 (fr) | 2016-12-21 | 2018-06-28 | Pi Industries Ltd. | Composés de 1,2,3-thiadiazole et leur utilisation en tant qu'agent de protection des cultures |
| UY37556A (es) | 2017-01-10 | 2018-07-31 | Bayer Ag | Derivados heterocíclicos como pesticidas |
| AU2018208422B2 (en) | 2017-01-10 | 2021-11-11 | Bayer Aktiengesellschaft | Heterocyclene derivatives as pest control agents |
| WO2018139560A1 (fr) | 2017-01-26 | 2018-08-02 | 三井化学アグロ株式会社 | Composé de pyridone et bactéricide à usage agricole et horticole utilisant celui-ci en tant que principe actif |
| WO2018138050A1 (fr) | 2017-01-26 | 2018-08-02 | Bayer Aktiengesellschaft | Dérivés hétérocycliques bicycliques condensés utilisés comme pesticides |
| TW201833107A (zh) | 2017-02-06 | 2018-09-16 | 德商拜耳廠股份有限公司 | 作為殺蟲劑之經2-(雜)芳基取代的稠合雜環衍生物 |
| EP3369320A1 (fr) | 2017-03-02 | 2018-09-05 | Bayer CropScience Aktiengesellschaft | Agent pour lutter contre les hémiptères |
| WO2018162312A1 (fr) | 2017-03-10 | 2018-09-13 | Basf Se | Dérivés spirocycliques |
| WO2018166855A1 (fr) | 2017-03-16 | 2018-09-20 | Basf Se | Dihydroisoxazoles à substitution hétérobicyclique |
| WO2018169045A1 (fr) | 2017-03-17 | 2018-09-20 | Meiji Seikaファルマ株式会社 | Agent de lutte contre l'acarien mésostigmates |
| BR112019020277B1 (pt) | 2017-03-28 | 2023-02-14 | Basf Se | Compostos, composição, método para combater ou controlar pragas de invertebrados, método para proteger plantas em crescimento, semente tratada, usos de um composto da fórmula i |
| MX2019011785A (es) | 2017-03-31 | 2019-11-18 | Basf Se | Proceso para preparar compuestos de 2,3-dihidrotiazolo[3,2-a]pirim idin-4-io quirales. |
| EP4298908A3 (fr) | 2017-03-31 | 2024-03-20 | Bayer Animal Health GmbH | Carboxamides tricycliques pour lutter contre les arthropodes |
| WO2018177993A1 (fr) | 2017-03-31 | 2018-10-04 | Bayer Cropscience Aktiengesellschaft | Pyrazoles pour lutter contre les arthropodes |
| WO2018190350A1 (fr) | 2017-04-10 | 2018-10-18 | 三井化学アグロ株式会社 | Composé pyridone, et bactéricide à usage agricole et horticole ayant ce composé pour principe actif |
| WO2018190351A1 (fr) | 2017-04-10 | 2018-10-18 | 三井化学アグロ株式会社 | Composé pyridone, et bactéricide à usage agricole et horticole ayant ce composé pour principe actif |
| TWI771402B (zh) | 2017-04-11 | 2022-07-21 | 日商三井化學Agro股份有限公司 | 吡啶酮化合物及以吡啶酮化合物作為有效成分的農園藝用殺菌劑 |
| KR20190138831A (ko) | 2017-04-12 | 2019-12-16 | 바이엘 악티엔게젤샤프트 | 살곤충제로서 사용하기 위한 메소이온성 이미다조피리딘 |
| RU2019136993A (ru) | 2017-04-20 | 2021-05-20 | Пи Индастриз Лтд. | Новые соединения фениламина |
| WO2018192793A1 (fr) | 2017-04-20 | 2018-10-25 | Basf Se | Dérivés de rhodanine substitués |
| WO2018192872A1 (fr) | 2017-04-21 | 2018-10-25 | Bayer Aktiengesellschaft | Imidazopyridines mésoioniques utilisées comme insecticides |
| US20200128830A1 (en) | 2017-04-24 | 2020-04-30 | Bayer Aktiengesellschaft | Fused bicyclic heterocycle derivatives as pesticides |
| MX2019012813A (es) | 2017-04-26 | 2020-01-14 | Basf Se | Derivados de succinimida sustituida como plaguicidas. |
| WO2018197401A1 (fr) | 2017-04-27 | 2018-11-01 | Bayer Animal Health Gmbh | Nouveaux dérivés bicycliques de pyrazole |
| TWI782983B (zh) | 2017-04-27 | 2022-11-11 | 德商拜耳廠股份有限公司 | 雜芳基苯基胺基喹啉及類似物 |
| CN110637019B (zh) | 2017-05-02 | 2022-07-12 | 拜耳公司 | 作为有害物防治剂的2-(杂)芳基-取代的稠合双环杂环衍生物 |
| EP3619213A1 (fr) | 2017-05-02 | 2020-03-11 | Bayer Aktiengesellschaft | Dérivés d'hétérocycles condensés à substitution 2-(hét)aryle utilisés comme pesticides |
| US20200275656A1 (en) | 2017-05-03 | 2020-09-03 | Bayer Aktiengesellschaft | Trisubstitutedsilylmethylphenoxyquinolines and analogues |
| EP3619220A1 (fr) | 2017-05-03 | 2020-03-11 | Bayer Aktiengesellschaft | Silylbenzylbenzimidazoles trisubstitués et analogues |
| JP2020518592A (ja) | 2017-05-03 | 2020-06-25 | バイエル・アクチエンゲゼルシヤフト | トリ置換シリルヘテロアリールオキシキノリン類及び類縁体 |
| HUE059057T2 (hu) | 2017-05-04 | 2022-10-28 | Bayer Cropscience Ag | 2-{[2-(feniloximetil)piridin-5-il]oxi}-etánamin-származékok és rokon vegyületek mint peszticidek, például növényvédelemre |
| WO2018202525A1 (fr) | 2017-05-04 | 2018-11-08 | Bayer Cropscience Aktiengesellschaft | Dérivés de phénoxyéthanamine pour lutter contre des organismes nuisibles |
| ES2910854T3 (es) | 2017-05-10 | 2022-05-13 | Basf Se | Compuestos pesticidas bicíclicos |
| WO2018224455A1 (fr) | 2017-06-07 | 2018-12-13 | Basf Se | Dérivés de cyclopropyle substitués |
| JP7157738B2 (ja) | 2017-06-08 | 2022-10-20 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| BR112019025331A2 (pt) | 2017-06-16 | 2020-06-23 | Basf Se | Compostos da fórmula (i), composição, métodos de proteção de safras e de combate, método não terapêutico de tratamento, semente, uso dos compostos e uso de composto |
| BR112019025191B1 (pt) | 2017-06-19 | 2023-11-28 | Basf Se | Compostos de pirimidínio substituídos, composição, método para proteger culturas, semente revestida, uso dos compostos e uso de um composto |
| WO2018234488A1 (fr) | 2017-06-23 | 2018-12-27 | Basf Se | Dérivés de cyclopropyle substitués |
| JP7210483B2 (ja) | 2017-06-30 | 2023-01-23 | バイエル・アニマル・ヘルス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 新規アザキノリン誘導体 |
| WO2019007888A1 (fr) | 2017-07-06 | 2019-01-10 | Bayer Aktiengesellschaft | Associations de principes actifs insecticides |
| WO2019007891A1 (fr) | 2017-07-06 | 2019-01-10 | Bayer Aktiengesellschaft | Associations de principes actifs insecticides |
| WO2019007887A1 (fr) | 2017-07-06 | 2019-01-10 | Bayer Aktiengesellschaft | Associations de principes actifs insecticides et fongicides |
| EP3284739A1 (fr) | 2017-07-19 | 2018-02-21 | Bayer CropScience Aktiengesellschaft | Composés (hét)aryl substitués comme produit de lutte contre les parasites |
| MX2020001403A (es) * | 2017-08-04 | 2020-03-09 | Bayer Animal Health Gmbh | Nuevos derivados de quinolina. |
| JP2020531420A (ja) | 2017-08-17 | 2020-11-05 | バイエル クロップサイエンス エルピーBayer Cropscience Lp | 液体肥料分散性組成物およびその方法 |
| WO2019038195A1 (fr) | 2017-08-22 | 2019-02-28 | Bayer Aktiengesellschaft | Dérivés hétérocycliques utilisés comme pesticides |
| WO2019042932A1 (fr) | 2017-08-31 | 2019-03-07 | Basf Se | Procédé de lutte contre les parasites du riz dans le riz |
| EP3453706A1 (fr) | 2017-09-08 | 2019-03-13 | Basf Se | Composés pesticides de l'imizazole |
| EP3684181B1 (fr) | 2017-09-20 | 2025-10-22 | Mitsui Chemicals Crop & Life Solutions, Inc. | Agent de lutte prolongée contre les ectoparasites pour un animal |
| WO2019068572A1 (fr) | 2017-10-04 | 2019-04-11 | Bayer Aktiengesellschaft | Dérivés hétérocycliques utilisés comme pesticides |
| US11399543B2 (en) | 2017-10-13 | 2022-08-02 | Basf Se | Substituted 1,2,3,5-tetrahydroimidazo[1,2-a]pyrimidiniumolates for combating animal pests |
| EP3473103A1 (fr) | 2017-10-17 | 2019-04-24 | Bayer AG | Concentré en suspension aqueux à base de 2-[(2,4-dichlorphényl)-méthyl]-4,4'-diméthyl-3-isoxazolidinone |
| CN111225562B (zh) | 2017-10-18 | 2022-08-02 | 拜耳公司 | 具有杀虫/杀螨特性的活性化合物结合物 |
| TWI791054B (zh) | 2017-10-18 | 2023-02-01 | 德商拜耳廠股份有限公司 | 具有殺昆蟲/殺蟎性質之活性化合物組合(五) |
| TW201930279A (zh) | 2017-10-18 | 2019-08-01 | 德商拜耳廠股份有限公司 | 具有殺昆蟲/殺蟎性質之活性化合物組合(三) |
| EP3697215B1 (fr) | 2017-10-18 | 2021-08-11 | Bayer Aktiengesellschaft | Combinaisons de composés actifs ayant des propriétés insecticides/acaricides |
| EP3473100A1 (fr) | 2017-10-18 | 2019-04-24 | Bayer Aktiengesellschaft | Combinaisons de composés actifs à propriétés insecticides/acaricides |
| CN111246742B (zh) | 2017-10-18 | 2022-09-23 | 拜耳公司 | 具有杀虫/杀螨特性的活性化合物结合物 |
| EP3689877A4 (fr) | 2017-11-03 | 2020-08-19 | South China Agricultural University | Composé tricyclique fusionné contenant de l'azote et son utilisation en tant qu'insecticide agro-forestier |
| BR112020009446A2 (pt) | 2017-11-13 | 2020-11-03 | Bayer Aktiengesellschaft | derivados de tetrazólio propila e seu uso como fungicida |
| BR112020010452A2 (pt) | 2017-11-28 | 2020-10-20 | Bayer Aktiengesellschaft | compostos heterocíclicos como pesticidas |
| WO2019121143A1 (fr) | 2017-12-20 | 2019-06-27 | Basf Se | Dérivés de cyclopropyle substitués |
| BR112020012614A2 (pt) | 2017-12-20 | 2020-11-24 | Pi Industries Ltd | compostos de fluoralquenil, processo de preparação e utilização |
| MX2020006566A (es) | 2017-12-21 | 2020-09-25 | Basf Se | Compuestos plaguicidas. |
| TW201927768A (zh) | 2017-12-21 | 2019-07-16 | 德商拜耳廠股份有限公司 | 三取代矽基甲基雜芳氧基喹啉及類似物 |
| IL275726B2 (en) | 2018-01-09 | 2024-06-01 | Basf Se | Silylethynyl hetaryl compounds as nitrification inhibitors |
| WO2019137995A1 (fr) | 2018-01-11 | 2019-07-18 | Basf Se | Nouveaux composés pyridazine destinés à la lutte contre les nuisibles invertébrés |
| EP3305786A3 (fr) | 2018-01-22 | 2018-07-25 | Bayer CropScience Aktiengesellschaft | Dérivés d'hétérocyclène bicycliques condensés en tant que pesticides |
| WO2019150311A1 (fr) | 2018-02-02 | 2019-08-08 | Pi Industries Ltd. | Composés de dithiol 1-3 et leur utilisation pour la protection de cultures contre des micro-organismes phytopathogènes |
| CN111836802A (zh) | 2018-02-12 | 2020-10-27 | 拜耳公司 | 杀真菌的*二唑 |
| WO2019162228A1 (fr) | 2018-02-21 | 2019-08-29 | Bayer Aktiengesellschaft | Dérivés de 1-(imidazol-1-yl à substitution en position 5)but-3-ène et leur utilisation en tant que fongicides |
| CN111741958A (zh) | 2018-02-21 | 2020-10-02 | 拜耳公司 | 作为害虫防治剂的稠合双环杂环衍生物 |
| PE20211754A1 (es) | 2018-02-28 | 2021-09-06 | Basf Se | Uso de compuestos de alcoxi pirazol funcionalizados con n como inhibidores de la nitrificacion |
| WO2019166558A1 (fr) | 2018-02-28 | 2019-09-06 | Basf Se | Utilisation d'éthers de pyrazole propargyle comme inhibiteurs de nitrification |
| BR112020016425A2 (pt) | 2018-02-28 | 2020-12-15 | Basf Se | Uso de composto de alcoxipirazol, composição para uso na redução da nitrificação, mistura agroquímica e métodos de redução da nitrificação e de tratamento de fertilizante ou composição |
| EP3765466B1 (fr) | 2018-03-12 | 2022-05-25 | Bayer Aktiengesellschaft | Dérivés d'hétérocyclène bicycliques condensés en tant que pesticides |
| WO2019175713A1 (fr) | 2018-03-14 | 2019-09-19 | Basf Corporation | Nouvelles molécules de catéchol et leur utilisation en tant qu'inhibiteurs de voies métaboliques associées à p450 |
| WO2019175712A1 (fr) | 2018-03-14 | 2019-09-19 | Basf Corporation | Nouvelles utilisations de molécules de catéchol en tant qu'inhibiteurs de voies métaboliques de glutathion s-transférase |
| WO2019185413A1 (fr) | 2018-03-27 | 2019-10-03 | Basf Se | Dérivés de cyclopropyle substitués pesticides |
| US20210147371A1 (en) | 2018-04-10 | 2021-05-20 | Bayer Aktiengesellschaft | Oxadiazoline derivatives |
| WO2019197615A1 (fr) | 2018-04-13 | 2019-10-17 | Bayer Aktiengesellschaft | Associations de principes actifs aux propriétés fongicides, insecticides et acaricides |
| MX2020010792A (es) | 2018-04-13 | 2020-10-28 | Bayer Ag | Combinaciones de ingredientes activos con propiedades insecticidas, fungicidas y acaricidas. |
| UY38184A (es) | 2018-04-17 | 2019-10-31 | Bayer Ag | Compuestos heteroarilo-triazol y heteroarilo-tetrazol novedosos como plaguicidas |
| BR112020019854A2 (pt) | 2018-04-20 | 2021-01-05 | Bayer Aktiengesellschaft | Compostos de heteroaril-triazol e heteroaril-tetrazol como pesticidas |
| CN111989328B (zh) | 2018-04-20 | 2023-04-18 | 拜耳公司 | 作为害虫防治剂的杂环衍生物 |
| CN108503559B (zh) * | 2018-04-23 | 2021-10-01 | 上海诗丹德生物技术有限公司 | 辣椒碱卤代衍生物的合成及其应用 |
| JP7403472B2 (ja) | 2018-05-09 | 2023-12-22 | バイエル・アニマル・ヘルス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 新規キノリン誘導体 |
| CN112423590B (zh) | 2018-05-15 | 2022-07-08 | 巴斯夫欧洲公司 | 包含benzpyrimoxan和oxazosulfyl的混合物和用途以及它们的施用方法 |
| WO2019224092A1 (fr) | 2018-05-22 | 2019-11-28 | Basf Se | Dérivés c15 à action pesticide de ginkgolides |
| WO2019224143A1 (fr) | 2018-05-24 | 2019-11-28 | Bayer Aktiengesellschaft | Combinaisons de substances actives à propriétés insecticides, nématicides et acaricides |
| CA3104880A1 (fr) | 2018-06-25 | 2020-01-02 | Bayer Cropscience Lp | Procede de traitement de semence |
| WO2020002189A1 (fr) | 2018-06-27 | 2020-01-02 | Bayer Aktiengesellschaft | Associations de principes actifs |
| WO2020002472A1 (fr) | 2018-06-28 | 2020-01-02 | Basf Se | Utilisation d'alkynylthiophènes en tant qu'inhibiteurs de nitrification |
| MA53085B1 (fr) | 2018-07-05 | 2022-12-30 | Bayer Ag | Thiophènecarboxamides substitués et analogues comme agents antibactériens |
| DK3826983T3 (da) | 2018-07-23 | 2024-08-05 | Basf Se | Anvendelse af substituerede 2-thiazoliner som nitrificeringshæmmere |
| US12151991B2 (en) | 2018-07-23 | 2024-11-26 | Basf Se | Use of a substituted thiazolidine compound as nitrification inhibitor |
| WO2020020813A1 (fr) | 2018-07-25 | 2020-01-30 | Bayer Aktiengesellschaft | Combinaisons de composés actifs fongicides |
| WO2020022412A1 (fr) | 2018-07-25 | 2020-01-30 | 三井化学アグロ株式会社 | Composé de pyridone et fongicide agricole et horticole comprenant celui-ci en tant que constituant actif |
| WO2020020816A1 (fr) | 2018-07-26 | 2020-01-30 | Bayer Aktiengesellschaft | Nouveaux dérivés de triazole |
| KR20210038617A (ko) | 2018-07-27 | 2021-04-07 | 바이엘 악티엔게젤샤프트 | 농약용 제어 방출 제제 |
| CA3107984A1 (fr) | 2018-07-31 | 2020-02-06 | Bayer Aktiengesellschaft | Formulations a liberation controlee contenant de la lignine pour produits agrochimiques |
| TW202009235A (zh) | 2018-08-17 | 2020-03-01 | 印度商皮埃企業有限公司 | 1,2-二硫醇酮化合物及其用途 |
| EP3613736A1 (fr) | 2018-08-22 | 2020-02-26 | Basf Se | Dérivés de glutarimide substitués |
| JP2022500412A (ja) | 2018-09-13 | 2022-01-04 | バイエル・アクチエンゲゼルシヤフト | 害虫防除剤としての複素環誘導体 |
| BR112021004865A2 (pt) | 2018-09-17 | 2021-06-01 | Bayer Aktiengesellschaft | uso do fungicida isoflucypram para controlar claviceps purpurea e reduzir esclerócios em cereais |
| KR102702570B1 (ko) | 2018-09-27 | 2024-09-04 | 미츠이 가가쿠 크롭 앤 라이프 솔루션 가부시키가이샤 | 수성 현탁상 농약 조성물 |
| US20220046925A1 (en) | 2018-09-28 | 2022-02-17 | Basf Se | Method of controlling pests by seed treatment application of a mesoionic compound or mixture thereof |
| EP3628157A1 (fr) | 2018-09-28 | 2020-04-01 | Basf Se | Procede de lutte contre les insectes resistants aux insecticides et transmission du virus aux plantes |
| EP3628158A1 (fr) | 2018-09-28 | 2020-04-01 | Basf Se | Composé pesticide contenant des substances mésoioniques et des biopesticides |
| EP3628156A1 (fr) | 2018-09-28 | 2020-04-01 | Basf Se | Procede de lutte contre les ravageurs de la canne a sucre, des agrumes, du colza et des plants de pomme de terre |
| WO2020070050A1 (fr) | 2018-10-01 | 2020-04-09 | Bayer Aktiengesellschaft | Dérivés d'imidazol-1-yl carbinol substitués en position 5 servant de fongicides |
| TW202028187A (zh) | 2018-10-18 | 2020-08-01 | 德商拜耳廠股份有限公司 | 吡啶基苯基胺基喹啉及類似物 |
| US20210387964A1 (en) | 2018-10-18 | 2021-12-16 | Bayer Aktiengesellschaft | Heteroarylaminoquinolines and analogues |
| TW202028193A (zh) | 2018-10-20 | 2020-08-01 | 德商拜耳廠股份有限公司 | 氧雜環丁基苯氧基喹啉及類似物 |
| EP3643711A1 (fr) | 2018-10-24 | 2020-04-29 | Bayer Animal Health GmbH | Nouveaux composés anthelminthiques |
| EP3643705A1 (fr) | 2018-10-24 | 2020-04-29 | Basf Se | Composés pesticides |
| WO2020109039A1 (fr) | 2018-11-28 | 2020-06-04 | Basf Se | Composés pesticides |
| PY1999323A (es) | 2018-11-28 | 2020-10-29 | Bayer Ag | (tio)amidas de piridazina como compuestos fungicidas |
| EP3620052A1 (fr) | 2018-12-12 | 2020-03-11 | Bayer Aktiengesellschaft | Utilisation d'alcools (1h-1,2,4-triazol-1-yl) substitués par des phenoxypyridinyles pour lutter contre des maladies provoquées par des champignons dans le maïs |
| AR117291A1 (es) | 2018-12-14 | 2021-07-28 | Syngenta Crop Protection Ag | Compuestos heterocíclicos de cianamida con actividad pesticida |
| WO2020126980A1 (fr) | 2018-12-18 | 2020-06-25 | Bayer Aktiengesellschaft | Combinaisons de composés actifs ayant des propriétés insecticides/acaricides |
| US20230031024A1 (en) | 2018-12-18 | 2023-02-02 | Basf Se | Substituted pyrimidinium compounds for combating animal pests |
| PY19106036A (es) | 2018-12-20 | 2021-07-06 | Bayer Ag | Compuestos de heterociclil piridazina como fungicidas |
| EP3669652A1 (fr) | 2018-12-21 | 2020-06-24 | Bayer AG | Combinaison de composés actifs |
| PY19106549A (es) | 2018-12-21 | 2021-07-13 | Bayer Ag | 1,3,4-oxadiazoles y derivados de éstos como nuevos agentes fungicidas |
| EP3679789A1 (fr) | 2019-01-08 | 2020-07-15 | Bayer AG | Combinaisons de composés actifs |
| EP3679790A1 (fr) | 2019-01-08 | 2020-07-15 | Bayer AG | Combinaisons de composés actifs |
| EP3679791A1 (fr) | 2019-01-08 | 2020-07-15 | Bayer AG | Combinaisons de composés actifs |
| EP3679793A1 (fr) | 2019-01-08 | 2020-07-15 | Bayer AG | Combinaisons de composés actifs |
| EP3679792A1 (fr) | 2019-01-08 | 2020-07-15 | Bayer AG | Combinaisons de composés actifs |
| EP3696177A1 (fr) | 2019-02-12 | 2020-08-19 | Basf Se | Composés hétérocycliques destinés à la lutte contre les organismes nuisibles invertébrés |
| WO2020169526A1 (fr) | 2019-02-18 | 2020-08-27 | Syngenta Crop Protection Ag | Composés hétérocycliques de cyanamide à action pesticide |
| US20220132851A1 (en) | 2019-03-01 | 2022-05-05 | Bayer Aktiengesellschaft | Active compound combinations having insecticidal/acaricidal properties |
| WO2020178307A1 (fr) | 2019-03-05 | 2020-09-10 | Bayer Aktiengesellschaft | Combinaison de composés actifs |
| WO2020182929A1 (fr) | 2019-03-13 | 2020-09-17 | Bayer Aktiengesellschaft | Urées et dérivés substitués en tant que nouveaux agents antifongiques |
| WO2020187656A1 (fr) | 2019-03-15 | 2020-09-24 | Bayer Aktiengesellschaft | Combinaisons de composés actifs ayant des propriétés insecticides/acaricides |
| CA3139524A1 (fr) | 2019-05-10 | 2020-11-19 | Bayer Cropscience Lp | Combinaisons de composes actifs |
| EP3769623A1 (fr) | 2019-07-22 | 2021-01-27 | Basf Se | Composés et dérivés mésoioniques d'imidazolium pour lutter contre les animaux nuisibles |
| EP3975718A1 (fr) | 2019-05-29 | 2022-04-06 | Basf Se | Composés imidazolium mésoioniques et leurs dérivés pour lutter contre les animaux nuisibles |
| WO2020254486A1 (fr) | 2019-06-21 | 2020-12-24 | Bayer Aktiengesellschaft | Hydroxyisoxazolines et leurs dérivés |
| WO2020256091A1 (fr) * | 2019-06-21 | 2020-12-24 | Meiji Seikaファルマ株式会社 | Formulation solide à base de flupyrimine pour la lutte contre les nuisibles du riz |
| WO2020254493A1 (fr) | 2019-06-21 | 2020-12-24 | Bayer Aktiengesellschaft | Thiénylhydroxyisoxazolines et leurs dérivés |
| EP3986876A1 (fr) | 2019-06-21 | 2022-04-27 | Bayer Aktiengesellschaft | Hydroxyisoxazolines et leurs dérivés |
| EP3986889A1 (fr) | 2019-06-21 | 2022-04-27 | Bayer Aktiengesellschaft | Oxadiazoles fongicides |
| EP3986877A1 (fr) | 2019-06-21 | 2022-04-27 | Bayer Aktiengesellschaft | Hydroxyisoxazolines et leurs dérivés |
| BR112021025264A2 (pt) | 2019-06-21 | 2022-01-25 | Bayer Ag | Fenoxifenil hidróxi-isoxazolinas e análogos como novos agentes antifúngicos |
| BR112021025333A2 (pt) | 2019-06-21 | 2022-05-24 | Bayer Ag | Benzilfenil hidróxi-isoxazolinas e análogos como novos agentes antifúngicos |
| EP3986892A1 (fr) | 2019-06-21 | 2022-04-27 | Bayer Aktiengesellschaft | Hydroxyisoxazolines et leur utilisation comme fongicides |
| MA56441B1 (fr) | 2019-07-03 | 2024-10-31 | Bayer Aktiengesellschaft | Carboxamides de thiophène substitués et leurs dérivés comme microbicides |
| EP3766879A1 (fr) | 2019-07-19 | 2021-01-20 | Basf Se | Dérivés de pytazole pesticides |
| TWI865563B (zh) | 2019-07-30 | 2024-12-11 | 德商拜耳動物保健有限公司 | 新穎異喹啉衍生物 |
| CN114615891A (zh) | 2019-09-11 | 2022-06-10 | 拜耳公司 | 基于2-[(2,4-二氯苯基)甲基]-4,4’-二甲基-3-异噁唑烷酮和苗前除草剂的高效制剂 |
| CN118496197A (zh) | 2019-12-20 | 2024-08-16 | 拜耳公司 | 取代的噻吩甲酰胺、噻吩甲酸及其衍生物 |
| EP4077317B1 (fr) | 2019-12-20 | 2024-06-26 | Bayer Aktiengesellschaft | Thienyloxazolones et analogues |
| WO2021131578A1 (fr) | 2019-12-27 | 2021-07-01 | 昭和電工株式会社 | Dispositif de production de gaz fluoré et détecteur à diffusion de lumière |
| EP3708565A1 (fr) | 2020-03-04 | 2020-09-16 | Bayer AG | Pyrimidinyloxyphénylamidines et leur utilisation comme fongicides |
| JP2023521342A (ja) | 2020-04-09 | 2023-05-24 | バイエル・アニマル・ヘルス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 駆虫性化合物としての置換縮合アジン類 |
| HUE069569T2 (hu) | 2020-04-16 | 2025-03-28 | Bayer Ag | Hatóanyag-kombinációk és azokat tartalmazó fungicid készítmények |
| WO2021209490A1 (fr) | 2020-04-16 | 2021-10-21 | Bayer Aktiengesellschaft | Cyclaminephénylaminoquinoléines utiles en tant que fongicides |
| EP4135523B1 (fr) | 2020-04-16 | 2024-09-25 | Bayer Aktiengesellschaft | Combinaisons de composés actifs et compositions de fongicide les comprenant |
| LT4135519T (lt) | 2020-04-16 | 2024-12-27 | Bayer Aktiengesellschaft | Veikliųjų medžiagų deriniai ir juos apimančios fungicidų kompozicijos |
| PL4135521T3 (pl) | 2020-04-16 | 2025-03-03 | Bayer Aktiengesellschaft | Kombinacje związków aktywnych i kompozycje grzybobójcze je zawierające |
| BR112022020857A2 (pt) | 2020-04-16 | 2022-11-29 | Bayer Ag | Combinações de compostos ativos e composições fungicidas compreendendo as mesmas |
| CN115915941B (zh) | 2020-05-06 | 2025-07-15 | 拜耳公司 | 作为杀真菌化合物的吡啶(硫代)酰胺 |
| BR112022023012A2 (pt) | 2020-05-12 | 2022-12-20 | Bayer Ag | (tio)amidas de triazina e pirimidina como compostos fungicidas |
| BR112022023550A2 (pt) | 2020-05-19 | 2023-01-03 | Bayer Cropscience Ag | (tio)amidas azabicíclicas como compostos fungicidas |
| CN115803320B (zh) | 2020-06-04 | 2025-07-15 | 拜耳公司 | 作为新的杀真菌剂的杂环基嘧啶类和杂环基三嗪类 |
| MX2022015625A (es) | 2020-06-10 | 2023-01-11 | Bayer Ag | Heterociclos sustituidos con azabiciclilo como nuevos fungicidas. |
| CN116157017A (zh) | 2020-06-18 | 2023-05-23 | 拜耳公司 | 作为杀菌剂用于作物保护的3-(哒嗪-4-基)-5,6-二氢-4h-1,2,4-噁二嗪衍生物 |
| UY39275A (es) | 2020-06-19 | 2022-01-31 | Bayer Ag | 1,3,4-oxadiazol pirimidinas como fungicidas, procesos e intermediarios para su preparación, métodos de uso y usos de los mismos |
| UY39276A (es) | 2020-06-19 | 2022-01-31 | Bayer Ag | Uso de compuestos de 1,3,4–oxadiazol–2–ilpirimidina para controlar microorganismos fitopatógenos, métodos de uso y composiciones. |
| WO2021255089A1 (fr) | 2020-06-19 | 2021-12-23 | Bayer Aktiengesellschaft | 1,3,4-oxadiazole pyrimidines et 1,3,4-oxadiazole pyridines utilisées comme fongicides |
| BR112022025692A2 (pt) | 2020-06-19 | 2023-02-28 | Bayer Ag | 1,3,4-oxadiazóis e seus derivados como fungicidas |
| WO2022058327A1 (fr) | 2020-09-15 | 2022-03-24 | Bayer Aktiengesellschaft | Urées et dérivés substitués en tant que nouveaux agents antifongiques |
| EP3915371A1 (fr) | 2020-11-04 | 2021-12-01 | Bayer AG | Combinaisons de composés actifs et compositions fongicides les comprenant |
| EP3915971A1 (fr) | 2020-12-16 | 2021-12-01 | Bayer Aktiengesellschaft | Phényl-s(o)n-phénylamidines et leur utilisation comme fongicides |
| WO2022129188A1 (fr) | 2020-12-18 | 2022-06-23 | Bayer Aktiengesellschaft | 1,2,4-oxadiazol-3-yl pyrimidines en tant que fongicides |
| WO2022129196A1 (fr) | 2020-12-18 | 2022-06-23 | Bayer Aktiengesellschaft | 1,2,4-oxadiazoles substitués par hétérobicycle utilisés en tant que fongicides |
| WO2022129190A1 (fr) | 2020-12-18 | 2022-06-23 | Bayer Aktiengesellschaft | 1,2,4-oxadiazoles substitués par (hétéro)aryle utilisés comme fongicides |
| JP7811947B2 (ja) | 2021-01-28 | 2026-02-06 | スペシャルティ オペレーションズ フランス | 農薬、微量栄養素及び着色剤の保持が改善されたイネ種子を処理するための方法 |
| CN116829521A (zh) | 2021-02-02 | 2023-09-29 | 巴斯夫欧洲公司 | Dcd和烷氧基吡唑作为硝化抑制剂的协同增效作用 |
| WO2022200364A1 (fr) | 2021-03-25 | 2022-09-29 | Syngenta Crop Protection Ag | Lutte contre les insectes, les acariens et les nématodes |
| EP4341245A1 (fr) | 2021-05-21 | 2024-03-27 | Basf Se | Utilisation de composés d'éthynylpyridine en tant qu'inhibiteurs de nitrification |
| EP4341248A1 (fr) | 2021-05-21 | 2024-03-27 | Basf Se | Utilisation d'un composé alcoxy pyrazole n-fonctionnalisé en tant qu'inhibiteur de nitrification |
| BR112023027004A2 (pt) | 2021-06-21 | 2024-03-12 | Basf Se | Estrutura de metal-orgânica, uso da estrutura de metal-orgânica, composição para uso na redução da nitrificação, mistura agroquímica e métodos de redução da nitrificação, de tratamento de fertilizante ou composição de fertilizante e de preparação de uma estrutura de metal-orgânica |
| WO2022268815A1 (fr) | 2021-06-24 | 2022-12-29 | Syngenta Crop Protection Ag | Lutte contre les insectes, les acariens et les nématodes nuisibles |
| WO2022268813A1 (fr) | 2021-06-24 | 2022-12-29 | Syngenta Crop Protection Ag | Lutte contre les insectes, les acariens et les nématodes nuisibles |
| EP4148052A1 (fr) | 2021-09-09 | 2023-03-15 | Bayer Animal Health GmbH | Nouveaux dérivés de quinoline |
| CA3234483A1 (fr) * | 2021-10-05 | 2023-04-13 | Upl Limited | Compositions et procede pour ameliorer de la sante des plantes et lutter contre les insectes |
| CN118541353A (zh) | 2021-11-03 | 2024-08-23 | 拜耳公司 | 作为杀真菌化合物的双(杂)芳基硫醚(硫代)酰胺 |
| WO2023092050A1 (fr) | 2021-11-20 | 2023-05-25 | Bayer Cropscience Lp | Combinaisons bénéfiques contenant des cellules de bacillus recombinées exprimant une sérine protéase |
| EP4441049A1 (fr) | 2021-11-30 | 2024-10-09 | Bayer Aktiengesellschaft | Bis(hétéro)aryl thioéther oxadiazines utilisées en tant que composés fongicides |
| US20250052673A1 (en) | 2021-12-15 | 2025-02-13 | Bayer Aktiengesellschaft | Spectroscopic solution for non-destructive quantification of one or more chemical substances in a matrix comprising coating and bulk material in a sample, such as coated seeds, using multivariate data analysis |
| EP4510830A1 (fr) | 2022-04-18 | 2025-02-26 | BASF Corporation | Formulations agricoles à charge élevée et procédés de fabrication associés |
| WO2023203066A1 (fr) | 2022-04-21 | 2023-10-26 | Basf Se | Action synergique en tant qu'inhibiteurs de nitrification d'oligomères de dicyandiamide (dcd) avec l'alcoxypyrazole et ses oligomères |
| CA3263381A1 (fr) | 2022-08-02 | 2024-02-08 | Basf Se | Composés pesticides pyrazolo |
| IT202200024963A1 (it) * | 2022-12-05 | 2024-06-05 | Angelini Pharma S P A | Composti attivatori dei canali potassio Kv7.2/Kv7.3 |
| CN115960043A (zh) * | 2023-01-30 | 2023-04-14 | 江西新龙生物科技股份有限公司 | 一种新烟碱杀虫剂及其合成方法 |
| EP4694887A1 (fr) | 2023-04-14 | 2026-02-18 | Elanco Animal Health GmbH | Prévention et/ou traitement à long terme d'une maladie par des inhibiteurs de slo-1 |
| WO2025031668A1 (fr) | 2023-08-09 | 2025-02-13 | Bayer Aktiengesellschaft | 4,5-dihydro-1h-2,4,5-oxadiazines à substitution azahétérobiaryle utilisés comme nouveaux fongicides |
| CN121693501A (zh) | 2023-08-09 | 2026-03-17 | 拜耳公司 | 作为新的杀菌剂的哒嗪-4-基噁二嗪 |
| CN122003403A (zh) | 2023-10-11 | 2026-05-08 | 拜耳公司 | 作为新杀菌剂的哒嗪-3-酮-4-基噁二嗪 |
| CN117658861A (zh) * | 2023-12-06 | 2024-03-08 | 宁夏大学 | 一种n、n-二取代氰胺衍生物的制备方法 |
| WO2025168620A1 (fr) | 2024-02-07 | 2025-08-14 | Bayer Aktiengesellschaft | 4,5-dihydro-1h-2,4,5-oxadiazines substituées par hétéroaryle utilisées en tant que nouveaux fongicides |
| WO2026078157A2 (fr) | 2024-10-10 | 2026-04-16 | Elanco Animal Health Gmbh | Modulateurs de slo-1 pour la prévention et/ou le traitement d'une maladie |
| WO2026078036A1 (fr) | 2024-10-11 | 2026-04-16 | Covestro (Netherlands) B.V. | Compositions polymères conduisant à une réduction de la poussière de graines et à une excellente fluidité des graines |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1285390A (en) * | 1969-12-23 | 1972-08-16 | Pharmacia Ab | Improvements in the n-alkylation of acylated amino compounds |
| US3867447A (en) * | 1972-08-25 | 1975-02-18 | Du Pont | Hydroxyguanidine O-carbamates |
| DE2342331A1 (de) | 1972-08-25 | 1974-03-14 | Du Pont | Mono- und disubstituierte hydroxyguanidine |
| US4203988A (en) * | 1975-11-12 | 1980-05-20 | Merck & Co., Inc. | Pyridinyl ureas and pharmaceutical use |
| US4206141A (en) * | 1978-12-15 | 1980-06-03 | Stauffer Chemical Company | Process for preparation of di-substituted cyanamides using quaternary salt catalysis |
| JPH07121909B2 (ja) | 1986-09-10 | 1995-12-25 | 日本バイエルアグロケム株式会社 | 新規複素環式化合物及び殺虫剤 |
| DE3639877A1 (de) | 1986-11-21 | 1988-05-26 | Bayer Ag | Hetarylalkyl substituierte 5- und 6-ringheterocyclen |
| JPS63227552A (ja) * | 1987-03-13 | 1988-09-21 | Shionogi & Co Ltd | 2−フルオロエチル誘導体、その製造法およびそれを有効成分とする有害生物防除剤 |
| JP2859301B2 (ja) * | 1989-07-08 | 1999-02-17 | 武田薬品工業株式会社 | 農園芸用殺虫組成物 |
| HU207047B (en) * | 1989-11-07 | 1993-03-01 | Richter Gedeon Vegyeszet | Process for producing new pyridine derivatives and pharmaceutical copositions comprising same |
| DE4021439A1 (de) * | 1989-12-14 | 1991-06-20 | Bayer Ag | 2-iminopyridin-derivate |
| JPH0578323A (ja) | 1991-03-11 | 1993-03-30 | Nippon Soda Co Ltd | 新規なヘテロ環化合物、その製造方法及び殺虫剤 |
| US5559108A (en) * | 1994-09-02 | 1996-09-24 | Bristol-Myers Squibb Company | Cephalosporin derivatives |
| US5804686A (en) | 1996-01-19 | 1998-09-08 | Neurogen Corporation | fused pyrrolecarboxamides; a new class of GABA brain receptor ligands |
| PT976737E (pt) | 1997-04-07 | 2009-07-31 | Nihon Nohyaku Co Ltd | Derivados de pirazole, processo para a sua preparação, produtos intermédios e agente de controlo de pragas que contém como ingrediente activo um desses derivados |
| JP3190859B2 (ja) | 1997-07-29 | 2001-07-23 | 松下電器産業株式会社 | Cdma無線送信装置及びcdma無線受信装置 |
| AU5415899A (en) * | 1998-07-16 | 2000-02-07 | Aventis Agriculture Ltd. | Aryl vinyl ether derivatives and their use as herbicides |
| DE10063486A1 (de) * | 2000-12-20 | 2002-07-04 | Bayer Ag | Dichlorpyridylmethylamide |
| JP2003026661A (ja) | 2001-06-27 | 2003-01-29 | Sinon Corp | 複素環化合物 |
| JP2005225860A (ja) * | 2003-11-11 | 2005-08-25 | Ishihara Sangyo Kaisha Ltd | ビフェニル誘導体又はその塩、それらを有効成分として含有する有害生物防除剤 |
| AR046698A1 (es) * | 2003-11-11 | 2005-12-21 | Ishihara Sangyo Kaisha | Derivado bifenilo o su sal, y pesticida que lo contienen como un ingrediente activo |
| DE102004018953A1 (de) | 2004-04-20 | 2005-11-17 | Bayer Cropscience Gmbh | 4-Halogenalkylpyridin-3-sulfonsäureamide, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel |
| DE102004041529A1 (de) * | 2004-08-27 | 2006-03-02 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Ketoenolen |
| US8604055B2 (en) * | 2004-12-31 | 2013-12-10 | Dr. Reddy's Laboratories Ltd. | Substituted benzylamino quinolines as cholesterol ester-transfer protein inhibitors |
| WO2006138148A1 (fr) * | 2005-06-13 | 2006-12-28 | Bayer Cropscience Ag | Dérivés pesticides de 5-bis(méthoxyméthyl)aminopyrazole |
| JP5152518B2 (ja) * | 2006-03-10 | 2013-02-27 | 日産化学工業株式会社 | 置換イソキサゾリン化合物及び有害生物防除剤 |
| ZA200810739B (en) | 2006-06-20 | 2010-03-31 | Ishihara Sangyo Kaisha | Pesticide containing novel pyridyl-methanamine derivative or its salt |
| JP5078323B2 (ja) | 2006-11-20 | 2012-11-21 | 株式会社カプコン | ゲーム装置、そのゲーム装置を実現するためのプログラム及び記録媒体 |
| JP4985025B2 (ja) | 2007-03-28 | 2012-07-25 | 凸版印刷株式会社 | マイクロニードルチップ集合体、マイクロニードルチップ、医療器具、マイクロニードルチップ集合体製造方法およびマイクロニードルチップ製造方法 |
| JP2008260691A (ja) * | 2007-04-10 | 2008-10-30 | Bayer Cropscience Ag | 殺虫性アリールイソオキサゾリン誘導体 |
| JP2008266230A (ja) * | 2007-04-23 | 2008-11-06 | Bayer Cropscience Ag | 殺虫性アリールピロリジン類 |
| WO2009038064A1 (fr) * | 2007-09-19 | 2009-03-26 | Institute Of Medicinal Molecular Design, Inc. | Dérivé hétérocyclique à activité inhibitrice sur la 11β-hydroxystéroïde déshydrogénase de type i |
| US7683064B2 (en) | 2008-02-05 | 2010-03-23 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
| MX2010007952A (es) * | 2008-02-07 | 2010-08-04 | Bayer Cropscience Ag | Arilpirrolinas insecticidas. |
| JP2010138082A (ja) * | 2008-12-09 | 2010-06-24 | Nippon Soda Co Ltd | 環状アミン化合物またはその塩、並びに有害生物防除剤 |
| PL2984930T3 (pl) * | 2010-08-31 | 2019-03-29 | Meiji Seika Pharma Co., Ltd. | Środek do zwalczania szkodników |
| EP3318554B1 (fr) * | 2011-08-26 | 2021-11-03 | Meiji Seika Pharma Co., Ltd. | Procédé de fabrication d'un agent de contrôle de nuisibles |
| CN112244015B (zh) * | 2012-02-29 | 2022-05-17 | 株式会社Mmag | 包括新型亚氨基吡啶衍生物的有害物防治组合物 |
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